Publication:
İns(22;?)(pter→q11.2

dc.authorscopusid59788593900
dc.authorscopusid55174210700
dc.authorscopusid6603455076
dc.authorscopusid21134879300
dc.contributor.authorElbistan, M.
dc.contributor.authorTekcan, A.
dc.contributor.authorKara, N.
dc.contributor.authorKoçak, I.
dc.date.accessioned2020-06-21T09:28:30Z
dc.date.available2020-06-21T09:28:30Z
dc.date.issued2012
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Elbistan] Mehmet, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Tekcan] Akin, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kara] Nurten, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Koçak] Idris, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractIn this study a woman that carried a familial ins (22;?) chromosome, applying to our laboratory with the aim of cytogenetic analysis after having two miscarriages and her mother who is also carrier of the same entity were investigated. Preparations obtained from the patient and her relatives by method of peripheric blood culture was banded by Trypsin Giemsa Banding (GTG) method after making her pedigree. The case had two miscarriages of two twins pregnancies that realized by the method of in vitro fertilisation, before application to our laboratory. The abortion sample taken from her second miscarriage, was investigated cytogenetically. Cytogenetic investigation showed 46,XX, ins(22;?)(pter→q11.2en_US
dc.identifier.doi10.5835/jecm.omu.29.04.012
dc.identifier.endpage318en_US
dc.identifier.issn1300-2996
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84882986557
dc.identifier.startpage316en_US
dc.identifier.urihttps://doi.org/10.5835/jecm.omu.29.04.012
dc.identifier.volume29en_US
dc.language.isotren_US
dc.relation.ispartofOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAbortionen_US
dc.subjectChromosomal Rearrangementen_US
dc.subjectInsertionen_US
dc.titleİns(22;?)(pter→q11.2en_US
dc.typeArticleen_US
dspace.entity.typePublication

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